EP2715611B1 - Systèmes et procédés de comptage de cellules - Google Patents

Systèmes et procédés de comptage de cellules Download PDF

Info

Publication number
EP2715611B1
EP2715611B1 EP12792944.6A EP12792944A EP2715611B1 EP 2715611 B1 EP2715611 B1 EP 2715611B1 EP 12792944 A EP12792944 A EP 12792944A EP 2715611 B1 EP2715611 B1 EP 2715611B1
Authority
EP
European Patent Office
Prior art keywords
sample
sample holder
cells
sensing system
cell counting
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP12792944.6A
Other languages
German (de)
English (en)
Other versions
EP2715611A4 (fr
EP2715611A1 (fr
Inventor
Daniel Y. Chu
Eli A. HEFNER
Yann Jouvenot
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bio Rad Laboratories Inc
Original Assignee
Bio Rad Laboratories Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bio Rad Laboratories Inc filed Critical Bio Rad Laboratories Inc
Publication of EP2715611A1 publication Critical patent/EP2715611A1/fr
Publication of EP2715611A4 publication Critical patent/EP2715611A4/fr
Application granted granted Critical
Publication of EP2715611B1 publication Critical patent/EP2715611B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10Investigating individual particles
    • G01N15/14Optical investigation techniques, e.g. flow cytometry
    • G01N15/1429Signal processing
    • G01N15/1433Signal processing using image recognition
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10Investigating individual particles
    • G01N2015/1006Investigating individual particles for cytology

Definitions

  • Cytometry is a technical specialty concerned with the counting and characterization of biological cells.
  • concentrations and relative numbers of red and white cells in a sample of a patient's blood may be of interest in assessing the patient's overall health, in diagnosing disease, or for other uses.
  • a blood sample may be placed into a sample holder, and a camera or other device having camera-like capabilities may take a digital photograph of the sample. An automated system may then analyze the digital photograph to identify and count the cells present and report the results.
  • US 2006/187442 discloses a method, comprising: capturing, using a sensing system, a first digital image of a first viewable portion of a sample containing cells; reconfiguring the sensing system and sample such that the sensing system images a second viewable portion of the sample, wherein the first and second viewable portions are arranged generally transversely with respect to a primary loading direction of the sample into a sample holder holding the sample; and capturing a second digital image of the second viewable portion.
  • GE Healthcare Application note 28-9673-96 AA IN Cell Analyzer 2000, 1 December 2009 discloses a method of counting cells, the method comprising: capturing, using a sensing system (IN Cell Analyzer 2000), a first digital image of a first viewable portion of a sample containing cells; analyzing, using a computerized analyzer, the first digital image to obtain a first count of the cells present in the first digital image; comparing the count with a threshold count; when the count is below the threshold count, reconfiguring the sensing system and sample such that the sensing system images a second viewable portion of the sample; capturing a second digital image of the second viewable portion; and analyzing the second digital image and reporting a test result based on the count of the cells present in the first and second digital images; and when the count is above the threshold count, reporting a text result based on a count of the cells present in the first digital image without capturing a second digital image.
  • a sensing system IN Cell Analyzer 2000
  • US Patent No. 4,171,866 discloses a sample holder, comprising: a body configures for insertion into a cell counting system; a plurality of windows in the body for receiving samples of one or more materials containing cells to be counted, the plurality of windows being arranged transversely or parallel with respect to a primary loading direction of the sample holder into the cell counting system. of one or more materials containing cells to be counted, the plurality of windows being arranged transversely or parallel with respect to a primary loading direction of the sample holder into the cell counting system.
  • EP-A-1764410 discloses a disk for storing liquid samples containing cells and for use in counting and observing through an optical microscope.
  • FIG. 1 illustrates a cell counting system 100 , in accordance with an embodiment of the invention.
  • a user may place a sample containing cells to be counted, for example a blood sample or other sample, into a sample holder 101.
  • Sample holder 101 may include a transparent window 102 into which the sample is dispersed for sensing as is described in more detail below.
  • window 102 may be formed from two closely-spaced transparent plates, between which the sample is dispersed.
  • a vent 105 may be provided to permit air to escape from between the plates as the sample enters.
  • the sample and its included cells disperse into window 102 from one edge, in primary loading direction 106.
  • Sample holder 101 may then be inserted into cell counting system 100, via slot 103.
  • Example cell counting system 100 preferably includes components for sensing an image of transparent window 102, and may also include elements for analyzing the image to determine the number of cells visible in the image. Test results may be presented to a user on a display 104.
  • FIG. 2 schematically illustrates a set of components that may be present in cell counting system 100.
  • sample holder 101 is disposed within a tray 201 that guides sample holder as it is inserted into cell counting system 100.
  • a spring 202 may be used to bias sample holder 101 toward one side of tray 201, for consistent registration.
  • a travel stop 203 limits the insertion of sample holder 101, and registers sample holder 101 at the correct insertion depth. It will be recognized that the features for holding and registering sample holder 101 shown in FIG. 2 are examples only, and that any suitable system for holding and registering sample holder 101 may be used.
  • a light source 204 illuminates at least a portion of window 102.
  • tray 201 may include a cutout portion (not visible in FIG. 2 ) that enables light from light source 204 to reach window 102.
  • Light source 204 may be any suitable kind of light source, for example a light emitting diode (LED), an incandescent light source, a fluorescent light source, or another kind of light source.
  • Light source 204 may be monochromatic, may emanate light in a narrow spectrum of wavelengths, or may emanate light in a broad spectrum.
  • a lens 205 projects an image of a viewing area 206 onto an array light sensor 207.
  • Viewing area 206 includes only a portion of window 102.
  • window 102 may be about 6 by 9 millimeters, while viewing area may be cover an area about 2 by 2 millimeters, although other dimensions may be used.
  • Array light sensor 207 may be a charge coupled device (CCD) sensor, a complementary metal oxide semiconductor (CMOS) sensor, or another kind of electronic image sensor. Such a sensor includes an array of light-sensitive sites called pixels. Each sensor pixel accumulates electric charge at a rate proportional to the intensity of light falling on the pixel. To read a digital image of viewing area 206, the sensor pixels may be reset, and the sensor exposed to light for a fixed time period. The amount of charge at each pixel is converted to a voltage, and the voltages are read and converted to numerical values. The digital image is an array of the numerical values representing the light intensities falling on the respective pixels. In some embodiments, color information may be gathered as well. In some embodiments, array light sensor 207 may include about 4 million pixels.
  • a controller 208 interacts with array light sensor 207 to gather the digital image.
  • the controller may provide timing signals to array light sensor 207, may provide configuration information, or other control signals.
  • Controller 208 also receives information indicating the light readings taken at the pixels.
  • the information may be in the form of analog voltages to be converted to digital values by controller 208, or may already have been converted to digital values at sensor 207.
  • Many different system architectures are possible for gathering digital images of viewing area 206.
  • a motor 209 or other actuator may also be present, as will be described in more detail below.
  • a focusing mechanism may be provided.
  • lens 205 or sensor 207 may be moved manually or automatically along the optical axis to achieve best focus.
  • FIG. 3 illustrates an example digital image 300 as may be taken by cell counting system 100 of viewing area 206, when a sample is present. About 52 cells 301 (only a few of which are labeled) are visible in image 300. In the array of numerical values that make up the digital image, the cells are present as associated groups of values that differ from values associated with the background 302 of the image. In some embodiments, the system utilizes a computerized method according to known techniques to locate and group the values that indicate the presence of cells, and counts the number of cells present in the image. In some embodiments, the system may also characterize the cells, for example counting live and dead cells separately, or distinguishing types of cells. In other embodiments, the images taken by the cell counting system may be simply displayed and the image analysis and cell counting may be performed manually.
  • the images taken by the cell counting system may be transferred to another system, for example a computer system, for analysis and cell counting.
  • images taken by the cell counting system may simply be viewed, without actually counting the cells, and it is intended that the appended claims encompass this use of the system.
  • FIG. 4 illustrates the relationship of viewing area 206 to window 102. Because the sample being measured has a relatively high concentration of cells, the number of cells found within viewing area 206 in relation to the area of viewing area 206 is representative of the concentration of the cells in the sample. That is, in this idealized example, the number of cells per unit area as measured in viewing area 206 is substantially the same as the number of cells per unit area as would be measured across all of window 102. Under these conditions, repeated tests of samples from the same source would likely give results with very little variation of the number of cells counted, in comparison to the number of counted cells.
  • FIG. 5 illustrates another example test of a sample having a much lower concentration of cells.
  • only seven cells appear within viewing area 206.
  • other areas of window 102 have cells clustered more closely together, so the number of cells counted within viewing area 206 may not be an accurate representation of the concentration of the sample. If this sample were to be tested again, it would be statistically likely that the cells in the second test would, by chance, disperse in a different way, and the number counted within viewing area 206 would be significantly different.
  • COV coefficient of variation
  • the standard deviation of the results of a number of tests on samples of a particular material
  • the mean of the test results.
  • COV indicates the variability of test results in relation to the magnitude of the mean result.
  • the multiplier of 100 is optional, and when used, expresses the results as a percentage. Materials with low cell concentrations may be especially susceptible to large COVs, in part because the denominator ⁇ in the expression for COV is small for materials with low cell concentrations. In general, it is desirable to reduce the variability of test results, whether measured by COV or another characteristic, so that the test results can be reported with confidence and repeated tests can be avoided.
  • FIG. 6 illustrates the operation of cell counting system 100 according to an example, not in accordance with the claims, useful for understanding the invention.
  • tray 201 is movable with respect to lens 205, so that the relative positions of sample holder 101 and the sensing system are variable.
  • tray 201 may be translated in direction 601 to position 201a, shown in broken lines.
  • Sample holder 101 is carried with tray 201 , such that the viewing area imaged by image sensor 207 encompasses area 206a of window 102.
  • Tray 201 may also be movable in the opposite direction to another position (not shown) in which the viewing area imaged by sensor 207 encompasses area 206b of window 102.
  • the movement of tray 201 may be accomplished by a motion system, which may include a motor such as motor 209 or another kind of actuator.
  • a motion system which may include a motor such as motor 209 or another kind of actuator.
  • the relative positions of the sensing system and sample holder 101 can be changed to a plurality of configurations, where the viewing area imaged by sensor 207 encompasses a different viewable portion of the sample holder in each configuration.
  • three different configurations are available, although it will be recognized that two configurations may be utilized, or more than three configurations may be available.
  • FIG. 7 illustrates the effect of the motion of tray 201, as seen at window 102.
  • the three areas 206, 206a, and 206b imaged by sensor 207 in the three configurations are shown superimposed on window 102.
  • controller 208 directs the sensing system to capture a digital image when the sample holder and sensing system are in each of the plurality of configurations, and the digital images are analyzed to count the cells present in the viewing area in all of the digital images. As can be seen in the example of FIG. 7 , this results in a larger effective measurement area, and a larger number of cells counted for the sample.
  • the larger effective measurement area reduces the likelihood that the cells in subsequent samples would disperse in such a way that the total number of counted cells would differ significantly in relation to the average number of counted cells. If COV is used as a measure of variability, the COV is reduced, as compared with a test using only a single image.
  • the system may perform a correlation operation to identify cells that appear in any overlap regions, to avoid double counting of cells.
  • tray 201 is moved in translation to expose different portions of window 102 to sensor 207.
  • motions resulting in rotation of sample holder 101 are instead used, optionally in combination with translation of the sample holder.
  • the relative positions of the sample holder and the sensing system move to a plurality of configurations such that the viewing area imaged by sensor 207 encompasses a different viewable portion of the sample holder in each configuration.
  • the cells may disperse into window 102 with a gradient in cell density.
  • cell distribution may be less dense in the portion of window 102 near the loading point, and more dense in portions of window removed from the loading point. That is, cell distribution may not be uniform as the window is traversed in the loading direction 106.
  • the transverse motion of sample holder 101 in gathering the multiple digital images may ensure that the portions of window 102 imaged by the system come from portions of window 102 with generally consistent cell distribution, and may further contribute to repeatability and accuracy of the test results, as compared with a system that moves the sample holder generally parallel to loading direction 106 .
  • the loading direction 106 of the sample into the sample holder is the same as the loading direction of the sample holder into the cell counting system.
  • the areas imaged are also preferably selected so that cell counts produced by the system are consistent with those produced by other methods.
  • the areas imaged by the system are centered about 6.3 millimeters from the window edge nearest loading point 701, as shown in FIG. 7 .
  • FIG. 8 illustrates a top view of motion of sample holder 101 according to the present invention.
  • sample holder 101 is inserted into a slot 103 in cell counting system 100.
  • the visible end 801 of sample holder 101 may be constrained from significant lateral translation by walls 803 of the enclosure of cell counting system 100.
  • Motion of tray 201 to expose multiple areas of window 102 to sensor 207 is provided by a rotational motion of tray 201 and sample holder 101.
  • tray 201 rotates about an axis 802 at slot 103. While axis 802 is positioned near the center of slot 103, other axes may be chosen, for example an axis at one edge of slot 103. In other embodiments, a rotational axis maybe used that is not near slot 103.
  • tray 201 when tray 201 is rotated to position 201c, shown in broken lines, then the viewing area imaged by image sensor 207 encompasses area 206c of window 102.
  • Tray 201 may also be rotated in the opposite direction to expose area 206d of window 102 to sensor 207. Because axis 802 is removed from window 102, the rotation of sample holder 101 results in a generally transverse change in the position of viewing area 206 with respect to window 102. Thus, areas 206, 206c, and 206d may all encompass portions of window 102 having similar cell distribution.
  • the axis of rotation of sample holder 101 is removed from viewing area 206 by a distance "R" that is at least 5 times the width "W" of viewing area 206, and more preferably by at least 8 times the width of viewing area 206.
  • the rotational axis may be removed by 10, 15, or more times the width of viewing area 206.
  • FIG. 9 illustrates a lower oblique view of one example motion system for providing the rotational motion illustrated in FIG. 8 .
  • rotation of motor 209 drives an eccentric pin 901, which in turn engages slot 902 in tray 201.
  • the motion of eccentric pin 901 drives slot 902, and consequently tray 201 and sample holder 101, to expose different areas of window 102 to sensor 207.
  • Motor 109 may be any suitable kind of motor, for example a stepper motor, a DC servo motor, or another kind of motor. Limit switches or other means may be provided for limiting the rotational travel of motor 109. In other embodiments, other kinds of actuators and motion systems may be utilized, for example a linear motor, a solenoid, a pneumatic or hydraulic actuator or another kind of actuator may drive tray 102 through gears, belts, pulleys, direct drive, friction drive, or another suitable mechanism.
  • FIG. 10 illustrates a flow chart of a method 1000 for counting cells, in accordance with an embodiment of the invention.
  • a digital image is captured of a first viewable portion of a sample containing cells to be counted.
  • the relationship of the a sensing system and the sample is reconfigured, such that the sensing system images a second viewable portion of the sample.
  • a second digital image is captured of the second viewable portion.
  • the first and second digital images are analyzed, and the cells detected in both of the digital images are counted.
  • a test result is reported that is based on the count of the cells in both the first and second images.
  • a count of 52 total cells may be reported.
  • other kinds of values based on the cell count may be reported.
  • the cell count may be converted to a concentration of cells, and the cell concentration may be reported.
  • each digital image being of a different viewable portion of the sample.
  • three, four, or more viewable areas and respective digital images may be utilized, and test results reported based on the combined count of cells appearing in all of the digital images.
  • the steps may be performed in any workable order. For example, both digital images may be captured before either is analyzed.
  • FIG. 11 illustrates a flow chart of a method 1100 for counting cells, in accordance with other embodiments.
  • counting the cells in a single digital image may be sufficient to give a concentration estimate that is repeatable and reliable.
  • further testing does not provide a significant advantage in accuracy or repeatability, and incurs additional testing time in reconfiguring the sensing system and sample, capturing an additional image, and analyzing the additional image.
  • Method 1100 recognizes that some tests may require analysis of only a single digital image to achieve satisfactory results, while other tests may require analysis of two or more digital images.
  • a first digital image is captured of a first viewable portion of a sample containing cells to be counted, and the digital image is analyzed to count the number of cells detected in the first digital image. This count represents an estimate of the concentration of cells in the sample.
  • the count is compared with a first threshold chosen to distinguish tests where analysis of a single digital image is sufficient to obtain a satisfactory concentration estimate and tests where multiple images are needed. If the count obtained from analysis of the first digital image exceeds the first threshold, a test result based on the cell count in the first digital image is reported at step 1103.
  • the sensing system and sample are reconfigured such that the sensing system images a second viewable portion of the sample.
  • a second digital image is captured of the second viewable portion of the sample, and the second digital image is analyzed to determine a cell count.
  • the combined count of cells detected in the first and second images is compared with a second threshold. If the combined count exceeds the threshold, a test result is reported in step 1107, based on the combined count of cells appearing in the first and second digital images. If the combined count does not exceed the second threshold, then the system is again reconfigured in step 1108, so that the sensing system images a third viewable portion of the sample.
  • a third digital image is captured of the third viewable area of the sample, and the third digital image is analyzed.
  • a test result is reported based on the combined cell count of all three images.
  • a plurality of digital images could be obtained of different viewing areas of the sample before any image analysis is performed.
  • a first one of the plurality of images may then be analyzed, and if the analysis indicates that enough cells were detected that additional testing is unnecessary, the result may be reported, analysis of any other digital images may be foregone, and any unused digital images discarded. If analysis of the first digital image indicates that the cell concentration was too low for a satisfactory result, then a second one of the plurality of digital images may be analyzed. If the analysis of the second digital image indicates that the first and second digital images provide satisfactory results, the results is reported, and analysis of any further images is foregone.
  • FIG. 12 illustrates one example architecture of a self-contained cell counting system such as system 100 illustrated in FIG. 1 .
  • controller 208 includes a processor 801.
  • Processor 801 may be any suitable kind of processor, such as a general purpose microprocessor or microcontroller.
  • Processor 801 accesses memory 802, which may comprise volatile memory and nonvolatile memory.
  • memory 802 may include nonvolatile memory, such as flash memory or programmable read-only memory, holding microprocessor instructions that, when executed by processor 801, cause controller to carry out its programmed functions.
  • Input/output module 803 may include one or more interfaces to other parts of the system, including motion system 804 (which may include motor 209 or another kind of actuator), image sensor 207, light source 204, and display 104.
  • memory 802 may hold instructions that cause processor 801 to direct the configuration of the system and the gathering of digital images, and may also include instructions for the analysis of the digital images to identify and count cells, and for reporting results.
  • FIG. 13 illustrates another example architecture of a cell counting system that includes an external computer system 1301.
  • controller 208 may transmit digital images captured by image sensor 207 to computer system 1301 for analysis and reporting of results.
  • tasks performed by cell counting systems according to embodiments of the invention may be allocated in any number of ways between hardware, software, and firmware, and between different internal processors and external computer systems. It is intended that the claims not be limited to any particular electronic architecture.
  • FIG. 14 illustrates a sample holder 1400 that may be conveniently used in conjunction with cell counting systems and methods according to embodiments of the invention.
  • Sample holder 1400 comprises a body 1401 that is configured for insertion into a cell counting system, for example a cell counting system as described above.
  • Sample holder 1400 also includes multiple windows 1402 into which samples may be placed.
  • Example sample holder 1400 includes four windows 1402, but more or fewer may be used.
  • the locations of windows 1402 correspond to the locations of viewing areas such as viewing area 206, which a cell counting system according to embodiments may present to a sensor such as sensor 207 for digital imaging.
  • an amount of a sample may be placed into one or more of windows 1402.
  • Sample holder 1400 may then be placed into a cell counting system according to an embodiment of the invention, and more than one of windows 1402 may be imaged.
  • the samples in the multiple windows being utilized may be of the same material or different materials, in any combination.
  • FIG. 15 shows an example of a sample holder 1500 that is not used in the present invention, the sample holder comprising a body 1501 and multiple windows 1502 arranged parallel to a primary loading direction 1503 of sample holder 1501 into a cell counting system.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Signal Processing (AREA)
  • Dispersion Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Computer Vision & Pattern Recognition (AREA)

Claims (15)

  1. Système de comptage de cellules (100), comprenant :
    un support d'échantillon (101) destiné à supporter un ensemble de cellules (301), dans lequel le support d'échantillon (101) a une direction de chargement primaire pour charger un échantillon comprenant l'ensemble de cellules (301) dans le support d'échantillon (101) ;
    un système de détection adapté pour produire une image numérique d'une zone de visualisation d'un support d'échantillon (101) ;
    un système de mouvement configuré pour changer les positions relatives du support d'échantillon (101) et du système de détection vers une pluralité de configurations, de telle sorte que la zone de visualisation (206) englobe une partie visualisable différente du support d'échantillon (101) dans chaque configuration, dans lequel les parties visualisables englobées sont agencées généralement transversalement par rapport à la direction de chargement primaire de l'échantillon dans le support d'échantillon (101) ;
    une enceinte configurée pour loger au moins une partie du système et définissant une fente (103) dans laquelle le support d'échantillon (101) est inséré, dans lequel la direction de chargement du support d'échantillon (101) dans l'enceinte du système de comptage de cellules (100) est la même que la direction de chargement primaire de l'échantillon dans le support d'échantillon (101), et
    dans lequel le système de mouvement est configuré pour faire tourner le support d'échantillon (101) tandis qu'une extrémité du support d'échantillon (101) reste entre des côtés de la fente (103) ; et
    un dispositif de commande (208) configuré pour diriger le système de détection afin de capturer une image numérique lorsque le support d'échantillon (101) et le système de détection sont dans chacune de la pluralité de configurations.
  2. Système de comptage de cellules (100) selon la revendication 1, comprenant en outre un analyseur informatisé configuré pour analyser les images numériques et compter les cellules (301) détectées dans la totalité des images numériques, de préférence le dispositif de commande (208) exécute la fonction de l'analyseur informatisé.
  3. Système de comptage de cellules (100) selon la revendication 1, comprenant en outre une source de lumière (204) configurée pour éclairer la zone de visualisation (206).
  4. Système de comptage de cellules (100) selon la revendication 1, dans lequel
    (i) les parties visualisables du support d'échantillon (101) sont situées dans une fenêtre unique (102) du support d'échantillon (101) ; ou
    (ii) les parties visualisables du support d'échantillon (101) sont situées dans différentes fenêtres (102) du support d'échantillon (101), de préférence les au moins deux fenêtres (102) contiennent des matériaux d'échantillon différents.
  5. Système de comptage de cellules (100) selon la revendication 1, dans lequel le système de mouvement est configuré pour faire tourner le support d'échantillon (101) dans un mouvement de basculement tandis qu'une extrémité du support d'échantillon (101) reste entre les côtés de la fente (103).
  6. Système de comptage de cellules (100) selon la revendication 5, dans lequel le système de rotation est configuré pour faire tourner le support d'échantillon (100) autour d'un point au niveau de la fente (103).
  7. Système de comptage de cellules (100) selon la revendication 1, dans lequel
    (i) les parties visualisables du support d'échantillon (101) englobées par la zone de visualisation (206) dans la pluralité de configurations ne se chevauchent pas ; ou
    (ii) la pluralité de configurations comprend au moins trois configurations.
  8. Système de comptage de cellules (100) selon la revendication 1, dans lequel le système de mouvement comprend un moteur configuré pour déplacer le support d'échantillon sous la commande du dispositif de commande.
  9. Système de comptage de cellules (100) selon la revendication 1, dans lequel le support d'échantillon (101) comprend en outre :
    un corps configuré pour une insertion dans la fente (103) ; et
    une pluralité de fenêtres (102) dans le corps pour recevoir des échantillons d'un ou de plusieurs matériaux contenant des cellules à compter, la pluralité de fenêtres (102) étant agencée dans la fente (103) transversalement ou parallèlement par rapport à la direction de chargement du support d'échantillon (101).
  10. Système de comptage de cellules (100) selon la revendication 9, dans lequel les fenêtres (102) sont espacées les unes des autres d'une distance correspondant à l'espacement des positions visualisables.
  11. Procédé (1000) de comptage de cellules, comprenant les étapes consistant à :
    charger un échantillon contenant un ensemble de cellules (301) dans un support d'échantillon (101), dans lequel le support d'échantillon (101) a une direction de chargement primaire dans laquelle l'échantillon est chargé dans le support d'échantillon ;
    insérer le support d'échantillon (101) dans un système de détection, dans lequel la direction de chargement du support d'échantillon (101) dans le système de détection est la même que la direction de chargement primaire de l'échantillon dans le support d'échantillon (101) ;
    capturer (1001), en utilisant le système de détection, une première image numérique d'une première partie visualisable de l'échantillon contenant les cellules (301) ;
    reconfigurer (1002) le système de détection et l'échantillon de telle sorte que le système de détection forme une image d'une deuxième partie visualisable de l'échantillon, dans lequel les première et deuxième parties visualisables sont agencées généralement transversalement par rapport à la direction de chargement primaire de l'échantillon dans un support d'échantillon (101) contenant l'échantillon, dans lequel la reconfiguration du système de détection et de l'échantillon comprenant une rotation du support d'échantillon (101) tandis qu'une extrémité du support d'échantillon (101) reste entre les côtés d'une fente (103) dans une enceinte qui loge au moins une partie du système de détection ; et
    capturer (1003) une deuxième image numérique de la deuxième partie visualisable.
  12. Procédé (1000) selon la revendication 11, comprenant en outre les étapes consistant à :
    analyser (1004), à l'aide d'un analyseur informatisé, les première et deuxième images numériques et compter les cellules (301) détectées dans les images numériques ; et
    rapporter (1005) un résultat de test sur la base du décompte des cellules (301) dans les première et deuxième images, et comprenant en outre facultativement les étapes consistant à :
    reconfigurer (1108) le système de détection et l'échantillon de telle sorte que le système de détection forme une image d'une troisième partie visualisable de l'échantillon ;
    capturer (1109) une troisième image numérique de la zone de visualisation ; et
    analyser la troisième image numérique et compter les cellules détectées dans la troisième image numérique ;
    dans lequel l'étape consistant à rapporter (1110) un résultat de test sur la base du décompte des cellules dans les première et deuxième images comprend l'étape consistant à rapporter un résultat de test sur la base du décompte des cellules dans les trois images numériques.
  13. Procédé (1000) selon la revendication 11, dans lequel
    (i) la première partie visualisable et la deuxième partie visualisable ne se chevauchent pas ; ou
    (ii) les première et deuxième parties visualisables sont situées dans une fenêtre unique (102) du support d'échantillon (101) ; ou
    (iii) les première et deuxième parties visualisables sont situées dans des fenêtres différentes (102) du support d'échantillon (101).
  14. Procédé (1000) selon la revendication 11, dans lequel
    (i) la reconfiguration du système de détection et de l'échantillon comprend un déplacement de l'échantillon ;
    (ii) la reconfiguration du système de détection et de l'échantillon comprend un déplacement d'au moins une partie du système de détection ; ou
    (iii) la reconfiguration du système de détection et de l'échantillon comprend un déplacement à la fois de l'échantillon et d'au moins une partie du système de détection.
  15. Procédé (1000) selon la revendication 11, dans lequel la reconfiguration (1002) du système de détection et de l'échantillon comprend une rotation du support d'échantillon (101) dans un mouvement de basculement.
EP12792944.6A 2011-05-31 2012-05-31 Systèmes et procédés de comptage de cellules Active EP2715611B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161491703P 2011-05-31 2011-05-31
US13/483,771 US9354155B2 (en) 2011-05-31 2012-05-30 Cell counting systems and methods
PCT/US2012/040251 WO2012166952A1 (fr) 2011-05-31 2012-05-31 Systèmes et procédés de comptage de cellules

Publications (3)

Publication Number Publication Date
EP2715611A1 EP2715611A1 (fr) 2014-04-09
EP2715611A4 EP2715611A4 (fr) 2014-12-03
EP2715611B1 true EP2715611B1 (fr) 2021-12-15

Family

ID=47259865

Family Applications (1)

Application Number Title Priority Date Filing Date
EP12792944.6A Active EP2715611B1 (fr) 2011-05-31 2012-05-31 Systèmes et procédés de comptage de cellules

Country Status (4)

Country Link
US (1) US9354155B2 (fr)
EP (1) EP2715611B1 (fr)
CN (1) CN103620619B (fr)
WO (1) WO2012166952A1 (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9001200B2 (en) 2010-01-12 2015-04-07 Bio-Rad Laboratories, Inc. Cell characterization using multiple focus planes
US8852524B2 (en) 2010-01-12 2014-10-07 Bio-Rad Laboratories, Inc. Cell counting slide with lateral reservoir for promoting uniform cell distribution
JP6194791B2 (ja) * 2013-12-27 2017-09-13 富士ゼロックス株式会社 画像処理装置及びプログラム
JP6586300B2 (ja) 2015-06-23 2019-10-02 オリンパス株式会社 細胞計数装置
KR102378607B1 (ko) * 2016-04-29 2022-03-24 배비스 인코포레이티드 신생아 스크리닝을 위한 출생 포인트 시스템 및 기기, 생화학 카트리지, 및 방법들
EP3321715B1 (fr) * 2016-11-11 2023-06-07 Mettler-Toledo Safeline Limited Procédé de test d'un appareil de détection de métaux et appareil de détection de métaux
CN117054316A (zh) * 2017-05-19 2023-11-14 兴盛生物科技股份有限公司 用于计数细胞的系统和方法
US11029268B2 (en) * 2017-08-06 2021-06-08 Clear-Cut Medical Ltd. Hybrid NMR and OCT system
CN109632609A (zh) * 2018-11-28 2019-04-16 合肥中元电气技术有限公司 一种计数精度高检测速度快的体细胞计数仪
CN109557013A (zh) * 2018-11-28 2019-04-02 合肥中元电气技术有限公司 一种用于液态奶体细胞检测系统平台机构
KR102148285B1 (ko) * 2019-01-18 2020-08-27 주식회사 바이오원 향상된 정확도와 컴팩트한 구조를 제공하는 셀카운터
CN109825427A (zh) * 2019-02-25 2019-05-31 广州牛顿光学研究院有限公司 一种全自动细胞活力分析系统
CN112113895A (zh) * 2019-06-21 2020-12-22 苏州中加康美科技有限公司 一种血细胞分析仪
BG67480B1 (bg) 2019-10-30 2022-12-15 "Милкотроник" Оод Устройство за диференциално броене на микрочастици в биологични течности
TWI740420B (zh) 2020-03-19 2021-09-21 邦睿生技股份有限公司 測試生物樣本品質確效試片及測試生物樣本品質檢測機之確效方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1764410A1 (fr) * 2005-09-16 2007-03-21 Effector Cell Institute, Inc. Disque et dispositif d'observation et comptage de cellules

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4171866A (en) 1978-04-20 1979-10-23 Tolles Walter E Disposable volumetric slide
US6718053B1 (en) * 1996-11-27 2004-04-06 Chromavision Medical Systems, Inc. Method and apparatus for automated image analysis of biological specimens
US20020098589A1 (en) 2001-01-19 2002-07-25 Crews Harold Richardson Multi-purpose reagent system and method for enumeration of red blood cells, white blood cells and thrombocytes and differential determination of white blood cells
KR100608498B1 (ko) * 2003-07-19 2006-08-08 주식회사 디지탈바이오테크놀러지 미세입자 계수 장치
EP1651947B1 (fr) * 2003-07-19 2015-11-04 NanoEnTek, Inc. Dispositif destine au comptage de microparticules
CA2659978A1 (fr) * 2006-08-04 2008-02-14 Ikonisys, Inc. Methode de traitement d'image pour un systeme de microscope
US8428331B2 (en) * 2006-08-07 2013-04-23 Northeastern University Phase subtraction cell counting method
US20120132313A1 (en) * 2006-08-25 2012-05-31 Anubha Bhatla Systems and methods for cutting materials
ITTO20070771A1 (it) * 2007-10-29 2009-04-30 Silicon Biosystems Spa Metodo e apparato per la identificazione e manipolazione di particelle
DK200801722A (en) * 2008-12-05 2010-06-06 Unisensor As Optical sectioning of a sample and detection of particles in a sample
JP2012531631A (ja) 2009-06-26 2012-12-10 バイオ−ラッド ラボラトリーズ,インコーポレイティド モジュラーマイクロスコープ構造
US8570370B2 (en) 2009-08-31 2013-10-29 Bio-Rad Laboratories, Inc. Compact automated cell counter
EP2491366B1 (fr) * 2009-10-20 2016-12-28 The Regents of The University of California Cellule holographique incohérente sans lentille et microscopie sur une puce
US8852524B2 (en) 2010-01-12 2014-10-07 Bio-Rad Laboratories, Inc. Cell counting slide with lateral reservoir for promoting uniform cell distribution
US9001200B2 (en) 2010-01-12 2015-04-07 Bio-Rad Laboratories, Inc. Cell characterization using multiple focus planes
US8609363B2 (en) 2010-11-18 2013-12-17 Bio-Rad Laboratories, Inc. Viability cell counting by differential light absorption

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1764410A1 (fr) * 2005-09-16 2007-03-21 Effector Cell Institute, Inc. Disque et dispositif d'observation et comptage de cellules

Also Published As

Publication number Publication date
EP2715611A4 (fr) 2014-12-03
CN103620619B (zh) 2017-12-29
WO2012166952A1 (fr) 2012-12-06
US9354155B2 (en) 2016-05-31
EP2715611A1 (fr) 2014-04-09
CN103620619A (zh) 2014-03-05
US20120314092A1 (en) 2012-12-13

Similar Documents

Publication Publication Date Title
EP2715611B1 (fr) Systèmes et procédés de comptage de cellules
US20200278341A1 (en) Method and apparatus for performing hematologic analysis using an array-imaging system for imaging and analysis of a centrifuged analysis tube
US11061031B2 (en) Dosimeters including lensless imaging systems
US8506901B2 (en) All-in-one specimen cup with optically readable results
US10488643B2 (en) Systems, devices, and methods for sample integrity verification
NO343728B1 (no) Måleapparat, fremgangsmåte og dataprogram
TW201741664A (zh) 具有放大功能的測試設備
CA3122235A1 (fr) Dispositif de collecte de solution avec element d'evaluation
JP2015510131A (ja) 試薬カード分析器の較正方法
US20230160832A1 (en) Biological sample quality apparatus
WO2017035513A1 (fr) Systèmes, dispositifs et procédés de vérification de l'intégrité d'échantillons

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20131125

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20141030

RIC1 Information provided on ipc code assigned before grant

Ipc: G06K 9/00 20060101AFI20141024BHEP

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

17Q First examination report despatched

Effective date: 20170518

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

RAP3 Party data changed (applicant data changed or rights of an application transferred)

Owner name: BIO-RAD LABORATORIES, INC.

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20210625

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602012077371

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: G06K0009000000

Ipc: G06V0010000000

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: DE

Ref legal event code: R081

Ref document number: 602012077371

Country of ref document: DE

Owner name: BIO-RAD LABORATORIES, INC., HERCULES, US

Free format text: FORMER OWNER: BIO-RAD LABORATORIES, INC., HERCULES, CA, US

Ref country code: GB

Ref legal event code: FG4D

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Ref country code: DE

Ref legal event code: R096

Ref document number: 602012077371

Country of ref document: DE

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 1456026

Country of ref document: AT

Kind code of ref document: T

Effective date: 20220115

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG9D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20211215

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220315

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1456026

Country of ref document: AT

Kind code of ref document: T

Effective date: 20211215

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220315

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220316

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220418

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602012077371

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20220415

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

26N No opposition filed

Effective date: 20220916

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20220531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230510

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20120531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20211215

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20240521

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240529

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20240527

Year of fee payment: 13